Disease #00378 (Caroli (Caroli disease), OMIM:600643)

Official abbreviation Caroli
Name Caroli disease
OMIM ID 600643
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2014-05-02 10:24:04 +02:00 (CEST)
Date last edited 2015-12-08 23:59:30 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00016545 - PubMed: Halbritter 2013 - ? ? Egypt ? - - - - Caroli 5y end-stage renal disease WDR19 WDR19 2 1 Heleen Arts
00016546 - PubMed: Halbritter 2013 - ? ? Oman ? - - - - Caroli polydactyly; retinal dystrophy; end-stage renal disease before 1y of age WDR19 WDR19 2 1 Heleen Arts
00016547 - PubMed: Halbritter 2013 - ? ? United States ? - - - - Caroli coritcal blindness; pancreatic cysts; hepatic cysts; end-stage renal disease <1y of age WDR19 WDR19 2 1 Heleen Arts
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.